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List of Altiazem Retard Active Pharmaceutical Ingredient (API) suppliers/manufacturers & exporters

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01 Jai Radhe Sales (1)

02 Fermion Oy (1)

03 LGM Pharma (1)

04 Cambrex Corporation (1)

05 Chemeca Drugs (1)

06 Credo Life Sciences (1)

07 DEAFARMA (1)

08 Darou Pakhsh Pharma Chem (1)

09 Divis Laboratories (1)

10 Fleming Laboratories (1)

11 Lusochimica SPA (1)

12 Nifty Labs (1)

13 Nishchem International Pvt. Ltd (1)

14 Osmopharm (1)

15 Pellets Pharma Limited (1)

16 Pellsys Pharma (1)

17 Piramal Pharma Solutions (1)

18 Qualitek pharma (1)

19 Spansules Pharma (1)

20 Teva API (1)

21 Titan Laboratories (1)

22 Zim Laboratories (1)

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01 DILTIAZEM HCL (2)

02 Diltiazem Hydrochloride (20)

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01 Finland (1)

02 India (13)

03 Iran (1)

04 Israel (1)

05 Italy (2)

06 Switzerland (1)

07 U.S.A (3)

- About The Company
Jai Radhe Sales was founded in 1999 as an out-of-the-box distribution firm specializing in the global supply of high-quality pharmaceutical ingredients. The firm provides complete sourcing solutions for pharmaceutical product...
Jai Radhe Sales was founded in 1999 as an out-of-the-box distribution firm specializing in the global supply of high-quality pharmaceutical ingredients. The firm provides complete sourcing solutions for pharmaceutical products from India, including technical and regulatory assistance. It believes in providing its customers with high-quality products at reasonable prices. It has always endeavored to achieve global standards in the field of pharmaceuticals and has carved out a niche for itself through new methods based on current market needs. Today, it has established itself as a truly global company, with exports to almost every continent.
Jai Radhe Sales

Cophex 2024

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- About The Company
Fermion is fully owned subsidiary of Orion Corporation & headquartered in Espoo, Finland. Together with Orion we are a fully integrated CDMO & offer services covering both APIs & Formulations. API portfolio consists of >30 ge...
Fermion is fully owned subsidiary of Orion Corporation & headquartered in Espoo, Finland. Together with Orion we are a fully integrated CDMO & offer services covering both APIs & Formulations. API portfolio consists of >30 generic APIs & >10 NCEs & 2 mfg. sites as well as R&D facilities are all located in Finland. Fermion has invested & expanded capabilities in the production of HPAPIs. Drug product CMO services include hormonal & non-hormonal semi-solids, cytotoxic oral solids & packaging. We have 3 mfg. sites & one packaging center for drug products at Orion.
- About The Company
LGM Pharma is a global leader in sourcing hard-to-find APIs and intermediates for the pharmaceutical and biotech industries. LGM is also a full service CDMO providing formulation, analytical method development and testing, an...
LGM Pharma is a global leader in sourcing hard-to-find APIs and intermediates for the pharmaceutical and biotech industries. LGM is also a full service CDMO providing formulation, analytical method development and testing, and commercial manufacturing. LGM Pharma offers custom API synthesis, analytical development, and regulatory services. With a network of over 300 accredited CGMP manufacturing partners, LGM provides unparalleled supply chain security. And, with over 100,000 square feet of FDA-inspected cGMP manufacturing and warehouse capacity, LGM Pharma provides a one-stop solution for solid dose, powder, semi-solid and liquid drugs.
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- About The Company
Driven by passion, our pharmaceutical products, expertise and technologies accelerate our customers’ small molecule therapeutics into markets across the world. With over 35 years of API development and manufacturing experti...
Driven by passion, our pharmaceutical products, expertise and technologies accelerate our customers’ small molecule therapeutics into markets across the world. With over 35 years of API development and manufacturing expertise, a growing team of more than 1,200 experts and a strong presence in the USA and Europe, we are tried and trusted across branded and generic API markets. We put all of our energy and experience into being your partner of choice. We create value for customers through manufacturing excellence, reliable quality and innovative science. Our people are the experts that our customers enjoy working with.
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- About The Company
Chemeca Drugs Private Limited was erstwhile M/s. Vegesna Laboratories Pvt Limited. M/s. Vegesna Laboratories Pvt Limited is a Private limited company having its Manufacturing Facility Unit at JN Pharmacity, Visakhapatnam esta...
Chemeca Drugs Private Limited was erstwhile M/s. Vegesna Laboratories Pvt Limited. M/s. Vegesna Laboratories Pvt Limited is a Private limited company having its Manufacturing Facility Unit at JN Pharmacity, Visakhapatnam established in the year 2008. Vegesna has become synonymous for its quality, deliveries, commitment & transparency making it a dependable & reliable partner to industry majors like DRL, Lupin, SUN PHARMA and Mylan by entering into long term strategic relationship for new products. We also provide contract manufacturing services for APIs and Intermediates.
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- About The Company
Credo Life one place for credibility, commitment, quality and delivery on time. Promoted by a dynamic team of techno-commercial professionals with decades of experience in the Pharmaceutical world. Our promoter’s moto is de...
Credo Life one place for credibility, commitment, quality and delivery on time. Promoted by a dynamic team of techno-commercial professionals with decades of experience in the Pharmaceutical world. Our promoter’s moto is deeply rooted in the belief of maintaining business ethics and to meet customer satisfaction. We know that the only way to achieve excellence in our company is to align our human resources with this objective. That is why we strive to surround ourselves with reliable people, of youthful spirit and honest heart, enterprising and perseverant.
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- About The Company
Darou Pakhsh Pharma Chem (DPPC Co.) as one of the qualified and leading producers of active pharmaceutical ingredients in the Iranian pharmaceutical industry started production since 1993 with GMP and ISO certificates. Daru...
Darou Pakhsh Pharma Chem (DPPC Co.) as one of the qualified and leading producers of active pharmaceutical ingredients in the Iranian pharmaceutical industry started production since 1993 with GMP and ISO certificates. Darupakhsh Pharmaceutical Chemistry Company with synthesis departments, clean and GMP spaces , glass line and steel reactors, separate warehouses for storage of raw materials, solvents, intermediates and final product and production units with advanced facilities and equipment at the final level and number 4 GMP dry clean section and quality control laboratory unit
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- About The Company
In the dinamic pharmaceutical field, DEAFARMA is the reference point for primaries Pharmaceutical Laboratories for over twenty years, even in the national and international territory. DEAFARMA works with success in the pharma...
In the dinamic pharmaceutical field, DEAFARMA is the reference point for primaries Pharmaceutical Laboratories for over twenty years, even in the national and international territory. DEAFARMA works with success in the pharmaceutical raw materials field through Agencies and professional relations with the most important European and Asiatic factories. Our partners are well known, reliable producers and all of them are operating in accordance with the latest GMP Rules. The APIs mentioned in the DEAFARMA catalogue are always supported by DMF and/or CEP.
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- About The Company
Divi's Laboratories Limited is a leading independent contract manufacturer of Active Pharmaceutical Ingredients and registered intermediates. We custom / exclusively manufacture for several Big Pharma companies under full cGM...
Divi's Laboratories Limited is a leading independent contract manufacturer of Active Pharmaceutical Ingredients and registered intermediates. We custom / exclusively manufacture for several Big Pharma companies under full cGMP. Customers regularly audit our facilities in areas of quality, EHS, business continuity etc. Unmatched Infrastructure:2 manufacturing sites. Both sites were successfully US-FDA Inspected No of DMFs 373 Pilot Plants30 Production Buildings39 Pharma Suites944 Reactors - 250 L to 30 KLTotal Capacity - 6676 M34 R&D Centers325 Scientists.
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- About The Company
Fleming Laboratories Limited is in the business of manufacturing and supply of high-quality generic Active Pharmaceutical Ingredients (APIs) to the global Pharmaceutical Industry. The facilities are audited & approved by /acc...
Fleming Laboratories Limited is in the business of manufacturing and supply of high-quality generic Active Pharmaceutical Ingredients (APIs) to the global Pharmaceutical Industry. The facilities are audited & approved by /accredited with various Regulatory agencies including EUGMP, EDQM, WHO GMP, PMDA (Japan), COFEPRIS (Mexico), Korea FDA.
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- About The Company
Lusochimica S.p.A. is an Italian manufacturer of bulk active ingredients for pharmaceuticals (API), having sales offices in Milan and two production plants in Lomagna and Pisa, whose production processes strictly comply with ...
Lusochimica S.p.A. is an Italian manufacturer of bulk active ingredients for pharmaceuticals (API), having sales offices in Milan and two production plants in Lomagna and Pisa, whose production processes strictly comply with international cGMP standards. Founded in 1964 and belonging to Menarini Group since 1984, Lusochimica S.p.A. incorporated former Laboratori Guidotti Fine Chemicals division starting January 2009, as a result of restructuring of Fine Chemicals operations within Menarini Group. Lusochimica’s mission is to dedicate our cutting edge manufacturing technology to ensure supplying high quality active ingredients to our clients because, according to our vision, safety of human drugs must be the driving force of our daily actions.
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- About The Company
The company was founded by a technocrat Mr. D. Kesava Reddy in the year 2005. The Managing Director Mr. D. Kesava Reddy along with other three Board of Directors involved in controlling the day to day operations of the compan...
The company was founded by a technocrat Mr. D. Kesava Reddy in the year 2005. The Managing Director Mr. D. Kesava Reddy along with other three Board of Directors involved in controlling the day to day operations of the company. The company has been focused on manufacturing and marketing of Bulk APIs (Bulk Drugs) and key Intermediates for APIs for Domestic and Global markets. About 60% is catered to domestic market and the rest 40% is catered to exports. The company does have a sister company named “Nifty Pharma Pvt. Ltd. located in Hyderabad focused on manufacturing & marketing of Semi-finished dosage forms.
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- About The Company
Public health is always an imperative that implies immense responsibility, not a mere re-adjustable option. As a company operating under world’s second largest industry of Pharmaceuticals, Nishchem International Pvt. Ltd. (...
Public health is always an imperative that implies immense responsibility, not a mere re-adjustable option. As a company operating under world’s second largest industry of Pharmaceuticals, Nishchem International Pvt. Ltd. (NIPL) stands on the virtue of revolutionizing the ends, as well as the means to safe and secure health. Medicinal drugs have always held an important place in the sphere of healing and treatment, with their applications ranging from diagnosis, treatment and cure right up to prophylaxis.
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- About The Company
Osmopharm S.A. is a GMP approved pharmaceutical company located in Switzerland and specialized in development and production of modified release solid oral form drugs under contract manufacturing.Our aim is to secure long ter...
Osmopharm S.A. is a GMP approved pharmaceutical company located in Switzerland and specialized in development and production of modified release solid oral form drugs under contract manufacturing.Our aim is to secure long term industrial productions for clients who register our formulation by themselves under their own brand (we are not the Marketing Authorization Holder).In order to support our clients with the registration, we can provide, under Secrecy and Supply Agreement, the technical documentation (Module 3 CTD dossier).For the time being we are not providing bioequivalence studies - those are in charge of the customers, if needed.
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- About The Company
Pellets Pharma Limited is a fast growing organization established by a team of professionals with over decades of experience in the pharmaceutical industry with specific reference to the development and manufacture of various...
Pellets Pharma Limited is a fast growing organization established by a team of professionals with over decades of experience in the pharmaceutical industry with specific reference to the development and manufacture of various modified release solid oral dosage forms. The company’s forte is the customized development and manufacturing of Modified Release Pellets / Retard Micro Granules of various Active Pharmaceutical Ingredients (APIs) including different combination blends in Ready - To - Fill form. The facility is designed to meet the regulatory requirements inline with the cGMP norms.
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- About The Company
Pellsys Pharma drives a new era of Value based Pharmaceutical deliverables. It is well recognized that several explicit, transparent, and consistent Production Standards including Quality aspects are in Vogue here. Pellsys p...
Pellsys Pharma drives a new era of Value based Pharmaceutical deliverables. It is well recognized that several explicit, transparent, and consistent Production Standards including Quality aspects are in Vogue here. Pellsys provides Superior Quality of pharmaceuticals where Clients are fully satisfied, The employees are proud of, and Stakeholders are Strategic Oriented.The Pellsys manufacturing facility – Machinery, plant and Warehousing exceeds GMP – Schedule M guidelines.Pellsys facilities are Company Owned over a 30,000+ SFT, Uber Modern structures with redundant facilities.
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Piramal Pharma Solutions (PPS) is a CDMO that provides end-to-end solutions for drug development and manufacturing across the drug life cycle to its clients in North America, Europe and Asia through a globally integrated netw...
Piramal Pharma Solutions (PPS) is a CDMO that provides end-to-end solutions for drug development and manufacturing across the drug life cycle to its clients in North America, Europe and Asia through a globally integrated network of facilities. It offers a range of services from drug discovery to commercial supply of APIs and finished dosage forms, along with specialized services like HPAPIs, antibody drug conjugations, sterile fill/finish, peptide products and services and potent solid oral drug products. PPS also provides services for biologics, including vaccines, gene therapies and monoclonal antibodies through its subsidiary Yapan Bio.
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Qualitek pharma is the one of selected few companies in India with dedicated state of art facilities for producing best quality Sustained and Modified Release Pellets, Taste Masked Granules. Qualitek pharma was established in...
Qualitek pharma is the one of selected few companies in India with dedicated state of art facilities for producing best quality Sustained and Modified Release Pellets, Taste Masked Granules. Qualitek pharma was established in the year 2005. Today Qualitek pharma has a manufacturing facility within the premises of Pharmaceuticals hub of Hyderabad.
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Spansules started in 2000 & now it is one of the leading pellets manufacturing pharmaceutical company with manufacturing facilities and R&D facilities spearheading landmark research in the area of Formulation Development. Spa...
Spansules started in 2000 & now it is one of the leading pellets manufacturing pharmaceutical company with manufacturing facilities and R&D facilities spearheading landmark research in the area of Formulation Development. Spansules is a WHO-GMP Certified Company with manufacturing practices and facilities that conform to that every Spansules product meets the most stringent quality standards. With all manufacturing facilities being supported by excellent infrastructure and compliance to the GMP requirements, Spansules has crossed numerous milestones in a comparatively short period of time.
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Teva API is a standalone business unit within Teva Pharmaceutical Industries, the world’s largest generic drug manufacturer. Employing over 4,000 professionals at 15 international plant sites and 6 R&D centers, Teva API is ...
Teva API is a standalone business unit within Teva Pharmaceutical Industries, the world’s largest generic drug manufacturer. Employing over 4,000 professionals at 15 international plant sites and 6 R&D centers, Teva API is a leading international supplier of active pharmaceutical ingredients (APIs) with the industry’s broadest portfolio of over 350 products. Its leadership in cutting-edge development, large-scale production capacity and global support make it an ideal API partner of choice. Over its more than 85 years of existence, Teva API has acquired and established top-rated manufacturing and development facilities around the world.
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- About The Company
Titan Laboratories is leading EU GMP approved Site for Sustained and Modified Release Pellets, Direct Compressible Granules, Tablets & Capsules.Our major focus in EU market is for1) CONTRACT MANUFACTURING SERVICES:-> As appro...
Titan Laboratories is leading EU GMP approved Site for Sustained and Modified Release Pellets, Direct Compressible Granules, Tablets & Capsules.Our major focus in EU market is for1) CONTRACT MANUFACTURING SERVICES:-> As approved Dossier Manufacturer.-> Site variation basis.-> cGMP pilot batch for BE/BA or Clinical Studies.2) CONTRACT RESEARCH SERVICES:-> Product Development - Generic Equivalent, Novel Sustained & Combination Products-> Method Development & Validation-> Dossier Preparation-> Stability Studies
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- About The Company
Incepted in 1989, Zim has made a significant mark as a maverick pharma innovator. Throughout all these years constantly penetrating newer areas of pharmaceutical technology and business, Zim has established itself as one of t...
Incepted in 1989, Zim has made a significant mark as a maverick pharma innovator. Throughout all these years constantly penetrating newer areas of pharmaceutical technology and business, Zim has established itself as one of the preferred healthcare solution provider in the field of new drug delivery systems. Headquartered in central India, in the industrial belt of Nagpur, we are a WHO GMP certified and ISO 9001:2008 accredited company supported by an excellent team of professionals and we have sufficient capacity to meet large requirements for different market segments. We are engaged in research and development, manufacturing, distribution and marketing of pharmaceutical dosage forms such as tablets, capsules, pellets, multi-particulate systems, dry syrups, directly compressible granules, taste masked powders, granules and orally disintegrating strips. At Zim we believe in constant innovation. We have earned appreciation for quality products and prompt services by domestic and international clients. Our business strategy is to innovate and deliver high-throughput technology based niche products. Zim is known in diverse, high-growth, niche markets, for institutional and pre-formulation intermediate businesses.
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Looking for 33286-22-5 / Diltiazem Hydrochloride API manufacturers, exporters & distributors?

Diltiazem Hydrochloride manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Diltiazem Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Diltiazem Hydrochloride manufacturer or Diltiazem Hydrochloride supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diltiazem Hydrochloride manufacturer or Diltiazem Hydrochloride supplier.

PharmaCompass also assists you with knowing the Diltiazem Hydrochloride API Price utilized in the formulation of products. Diltiazem Hydrochloride API Price is not always fixed or binding as the Diltiazem Hydrochloride Price is obtained through a variety of data sources. The Diltiazem Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Diltiazem Hydrochloride

Synonyms

33286-22-5, Diltiazem hcl, Cardizem, Dilzem, Dilzene, Masdil

Cas Number

33286-22-5

Unique Ingredient Identifier (UNII)

OLH94387TE

About Diltiazem Hydrochloride

A benzothiazepine derivative with vasodilating action due to its antagonism of the actions of CALCIUM ion on membrane functions.

Altiazem Retard Manufacturers

A Altiazem Retard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Altiazem Retard, including repackagers and relabelers. The FDA regulates Altiazem Retard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Altiazem Retard API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Altiazem Retard manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Altiazem Retard Suppliers

A Altiazem Retard supplier is an individual or a company that provides Altiazem Retard active pharmaceutical ingredient (API) or Altiazem Retard finished formulations upon request. The Altiazem Retard suppliers may include Altiazem Retard API manufacturers, exporters, distributors and traders.

click here to find a list of Altiazem Retard suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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